Integra NeuroSciences recalls Codman Microsensor Basic Kit (Catalog 626631US) due to potential corrosion stains on the 14-gauge Tuohy Needle. This may affect subdural and intraparenchymal pressure monitoring.
Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.
Integra NeuroSciences is recalling the Codman Microsensor Basic Kit (Catalog Number 626631US) because the 14-gauge Tuohy Needle included in the kit may develop corrosion stains. This could potentially interfere with medical procedures requiring intracranial pressure monitoring.
Corrosion stains on the 14-gauge Tuohy Needle could potentially interfere with the accuracy of intracranial pressure monitoring. This may affect the proper functioning of the Microsensor and Cerelink ICP Kits used in medical procedures.
Patients using the Codman Microsensor Basic Kit for subdural or intraparenchymal pressure monitoring are most at risk. The recall applies to specific lot numbers and catalog numbers.
Check for the Catalog Number 626631US on the kit. The affected lots include specific numbers listed in the recall notice, such as 7288007, 7288040, and others.
Look for the Catalog Number 626631US on the Codman Microsensor Basic Kit packaging.
The recall is due to potential corrosion stains on the 14-gauge Tuohy Needle included in the kit, which could interfere with intracranial pressure monitoring.
The official recall notice does not specify a remedy or action for affected kits.
Affected lot numbers include 7288007, 7288040, 7294017, and others as listed in the recall notice.
We’ve drafted a message you can send Integra NeuroSciences to request your refund or repair — edit it as you like.
Subject: Recall Z-1036-2026 — Integra NeuroSciences Integra NeuroSciences Hello, I own a Integra NeuroSciences that is covered by recall Z-1036-2026 from Integra NeuroSciences. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
